Improvement of insulin resistance and early atherosclerosis in patients after gastric banding

Obes Res. 2004 Feb;12(2):284-91. doi: 10.1038/oby.2004.36.

Abstract

Objective: To evaluate the effect of massive weight loss on insulin sensitivity, soluble adhesion molecules, and markers of the insulin resistance syndrome (IRS).

Research methods and procedures: Eighteen morbidly obese patients underwent gastric banding and were evaluated before and 6 and 12 months after surgery. Total insulin secretion, hepatic insulin extraction, and insulin sensitivity were analyzed by oral glucose-tolerance test model analysis. In addition, soluble intercellular adhesion molecule-1, vascular cell adhesion molecule-1, E-selectin, leptin, high-sensitivity C-reactive protein, plasminogen activating factor-1 (PAI-1), and tissue plasminogen activator were measured.

Results: BMI dropped from 45.22 +/- 5.62 to 36.99 +/- 4.34 kg/m(2) after 6 months and 33.72 +/- 5.55 kg/m(2) after 12 months (both p < 0.0001). This intervention resulted in a significant reduction of blood pressure (p < 0.00001), triglycerides (p < 0.01), fasting blood glucose (p = 0.03), basal insulin (p < 0.001), and basal C-peptide (p = 0.008) levels. Total insulin secretion decreased (p < 0.05), whereas hepatic insulin extraction (p < 0.05) and oral glucose insulin sensitivity index (p < 0.0001) increased compared with baseline. Leptin (p < 0.0001) and E-selectin levels decreased significantly after 6 and 12 months (p = 0.05), whereas significantly lower levels of intercellular adhesion molecule-1 and PAI-1 were only seen after 6 months. Subclinical inflammation, measured by high-sensitivity C-reactive protein, was lowered to normal ranges. No changes were observed in vascular cell adhesion molecule-1 and tissue plasminogen activator levels.

Discussion: Although gastric banding ameliorates several features of the IRS, including 29.05% improvement in insulin sensitivity and blood pressure and reduction of soluble adhesion molecules and PAI-1, considerable weight loss did not normalize all components of the IRS in morbidly obese patients.

MeSH terms

  • Adult
  • Arteriosclerosis / blood*
  • Arteriosclerosis / rehabilitation
  • C-Peptide / blood
  • Cell Adhesion Molecules / blood
  • E-Selectin / blood
  • Female
  • Glucose Tolerance Test
  • Humans
  • Hypertension / therapy
  • Insulin / metabolism*
  • Insulin Resistance / physiology*
  • Intercellular Adhesion Molecule-1 / blood
  • Leptin / blood
  • Male
  • Obesity, Morbid / blood*
  • Obesity, Morbid / rehabilitation
  • Obesity, Morbid / surgery
  • Plasminogen Activators / blood
  • Stomach / surgery
  • Vascular Cell Adhesion Molecule-1 / blood
  • Weight Loss / physiology*

Substances

  • C-Peptide
  • Cell Adhesion Molecules
  • E-Selectin
  • Insulin
  • Leptin
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Plasminogen Activators